JAMA news releases are made available to the public after 3 pm US Central time on the first 4 Tuesdays of each month. The Archives Journals news releases are made available to the public after 3 pm Central time on Mondays. We also provide a list of previous news releases.
THIS WEEK'S CONTENT
JAMA NEWS RELEASES
(Embargoed for Release: 3 p.m. CT, Tuesday, August 17, 2004)
JAMA NEWS RELEASES
ADOLESCENTS WITH DEPRESSION OFTEN RESPOND WELL TO COMBINATION OF ANTIDEPRESSANT AND COGNITIVE BEHAVIORAL THERAPY
SURVIVAL RATES IMPROVE FOR SOME MEN WITH PROSTATE CANCER WHEN COMBINATION THERAPIES USED
VITAMIN E SHOWS MIXED EFFECTS AGAINST RESPIRATORY INFECTIONS IN NURSING HOME RESIDENTS
INFORMATION CONTAINED IN THESE NEWS RELEASES IS PROTECTED BY COPYRIGHT. JOURNAL ATTRIBUTION IS REQUIRED.
TV Note: This week's JAMA video news release is on therapy for adolescents with depression. The release will be fed Tuesday, August 17, from 9:00 - 9:30 a.m. ET on Intelsat America 6 (formerly Telstar 6), Transponder 11 (C-Band) and from 2:00 - 2:30 p.m. ET on Intelsat America 6, Transponder 11 (C-Band). For more information, call 312/464-JAMA (5262).
Please Note: Our e-mail has changed to
mediarelations{at}jama-archives.org
JOURNALISTS CAN NOW ACCESS EMBARGOED JAMA/ARCHIVES STUDIES ONLINE
Go to www.jamamedia.org for more information and to apply for access.
Please Note: The FOR THE MEDIA Web site now has a search feature to enable media to find previous JAMA/Archives news releases on specific medical topics. This search feature link is located on the home page at www.jamamedia.org
Embargoed for Release: 3 p.m. CT, TUESDAY, August 17, 2004
Media Advisory: To contact John S. March, M.D., M.P.H., call Tracey Koepke at 919-660-1301.
To contact editorial author Richard M. Glass, M.D., call Jann Ingmire at 312-464-2499.
ADOLESCENTS WITH DEPRESSION OFTEN RESPOND WELL TO COMBINATION OF ANTIDEPRESSANT AND COGNITIVE BEHAVIORAL THERAPY
CHICAGOAdolescents with major depressive disorder showed improvement after treatment that combined fluoxetine (an antidepressant medication) and cognitive behavioral therapy (CBT), according to the results of the Treatment for Adolescents with Depression Study (TADS) published in the August 18 issue of JAMA, the Journal of the American Medical Association.
According to background information in the article, major depressive disorder (MDD) is common in adolescence. "...depression in adolescence is a major risk factor for MDD, suicide, and long-term psycho-social impairment in adulthood. Thus, improvements in the treatment of MDD among adolescents should positively affect public health."
John S. March, M.D., M.P.H., from Duke University Medical Center, Durham, N.C., and colleagues from the TADS team, evaluated the effectiveness of four treatments among adolescents with MDD. This study included 439 patients with a primary diagnosis of MDD who ranged in age from 12 to 17 years. They enrolled in the study between spring 2000 and summer 2003 at 13 academic and community clinics across the United States. The participants were randomly assigned to twelve weeks of fluoxetine alone, CBT alone, CBT with fluoxetine, or placebo (sugar pill). "In TADS, CBT is a skills-oriented treatment based on the assumption that depression is caused by or maintained by depressive thought patterns and a lack of active, positively reinforcing behavioral patterns; treatment included 15 sessions, which lasted between 50 and 60 minutes, over the first 12 weeks," the authors describe.
"Compared with fluoxetine alone and CBT alone, treatment [combining] fluoxetine with CBT was superior," the authors report. "Fluoxetine alone is a superior treatment to CBT alone. Rates of response for fluoxetine with CBT were 71 percent; fluoxetine alone, 60.6 percent; CBT alone, 43.2 percent; and placebo, 34.8 percent. ...Clinically significant suicidal thinking, which was present in 29 percent of the sample at baseline, improved significantly in all 4 treatment groups. Fluoxetine with CBT showed the greatest reduction. Seven (1.6 percent) of 439 patients attempted suicide; there were no completed suicides." The researchers also found treatment with fluoxetine alone elevated the risk for psychiatric adverse events. "While fluoxetine did not appear to increase suicidal ideation [thoughts], harm-related adverse events may occur more frequently in fluoxetine-treated patients and CBT may protect against these events," the researchers add.
In conclusion the authors write: "First, given the high prevalence, morbidity, and significant mortality associated with MDD, the identification of depressed adolescents and provision of evidence-based treatment should be mandatory in health care systems. Second, despite calls to restrict access to medications, medical management of MDD with fluoxetine, including careful monitoring for adverse events, should be made widely available, not discouraged. Third, given incremental improvement in outcome when CBT is combined with medication and, as importantly, increased protection from suicidality, CBT also should be readily available as part of comprehensive treatment for depressed adolescents."
(JAMA. 2004;292:807-820. Available post-embargo at jama.com)
Editor's Note: The research for this article was supported by a contract from the National Institute of Mental Health. Lilly Inc. provided fluoxetine and matching placebo under an independent educational grant to Duke University. Please see JAMA study for authors' financial disclosures.
EDITORIAL: TREATMENT OF ADOLESCENTS WITH MAJOR DEPRESSION
In an accompanying editorial, Richard M. Glass, M.D., Deputy Editor, JAMA, and the Department of Psychiatry, University of Chicago, writes, "the publication of the results of the Treatment for Adolescents With Depression Study (TADS) in this issue of JAMA is certainly timely in view of recent and widely publicized controversies regarding treating adolescents with depression.
"...the TADS results raise a mixture of questions and answers regarding the complicated issue of whether antidepressant drug treatment prescribed to treat depression might increase the risk for depression's most dangerous outcome, suicidal behavior. The reduction of suicidal ideation over time is reassuring, but the increased risk for harm-related adverse events observed in the patients receiving fluoxetine suggests that the increase in activation, irritability, or disinhibition sometimes associated with SSRI [selective serotonin reuptake inhibitor] treatment warrants careful monitoring in clinical practice. However, the TADS results leave this as a question rather than a firm answer because those specific symptoms were rare among the patients receiving fluoxetine."
"Probably the most important message from TADS is that carefully assessed, empirically validated treatments are available for adolescents with major depression. A corollary of that message is that depressive illness is a major public health problem with substantial morbidity and mortality for adolescents as well as for adults. The results from this major new trial demonstrate that although treatment of a depressive illness is often successful and gratifying for patients and clinicians, such success typically requires more than a brief visit for prescription of medication. Rather, it requires careful assessment and monitoring in the context of an ongoing patient-physician relationship. Furthermore, the current evidence suggests that the likelihood of a good outcome is enhanced by the combination of appropriate and carefully monitored drug treatment with an empirically validated psychotherapy."
(JAMA. 2004;292:861-863. Available post-embargo at jama.com)
For More Information: Contact the JAMA/Archives Media Relations Department at 312/464-JAMA (5262) or email: mediarelations{at}jama-archives.org (please note new email address).
Go back to the top.
Embargoed for Release: 3 p.m. CT, TUESDAY, August 17, 2004
Media Advisory: To contact Anthony V. D'Amico, M.D., Ph.D., call Melanie Franco at 617-534-1605. To contact editorial author Theodore L. DeWeese, M.D., call Vanessa Wasta at 410-955-1287.
SURVIVAL RATES IMPROVE FOR SOME MEN WITH PROSTATE CANCER WHEN COMBINATION THERAPIES USED
CHICAGOThe addition of six months of androgen suppression therapy (AST) to radiation therapy improves survival of patients with clinically localized prostate cancer, according to a study in the August 18 issue of JAMA, the Journal of the American Medical Association.
"Combining three years of AST with 70 Gy RT (dose of radiation therapy) has been shown to improve survival rates for patients with locally advanced prostate cancer," the authors provide as background information. "However, the toxicity of long-term AST can be significant, particularly in elderly patients." AST is a treatment that inhibits the release of androgen, the male sex hormone.
Anthony V. D'Amico, M.D., Ph.D., from Brigham and Women's Hospital, Boston, and colleagues, assessed the survival benefit of 3-dimensional conformal radiation therapy (3D-CRT) alone or in combination with 6 months of AST in patients with clinically localized prostate cancer. The 206 patients were randomized to receive 70 Gy 3D-CRT alone (n=104) or in combination with 6 months of AST (n = 102) from December 1, 1995 to April 15, 2001. The patients included those with a prostate specific antigen (PSA) of at least 10 ng/mL, a Gleason score (grading system for prostate cancer) of at least 7, or radiographic evidence of disease outside the prostate. Follow-up visits were performed at the end of radiation treatment every 3 months for 2 years, every 6 months for an additional 3 years, and then annually until death or January 15, 2004, the end of the study.
"After a median (midpoint) follow-up of 4.52 years, patients randomized to receive 3D-CRT plus AST had significantly higher survival, lower prostate cancer-specific mortality [death], and higher survival free of salvage AST [salvage treatment is used when cancer recurs after initial treatment]," the authors found. Standardized estimates of 5-year survival rates were 88 percent in the 3D-CRT plus AST group vs. 78 percent in the 3D-CRT group. Rates of survival free of salvage AST at 5 years were 82 percent in the 3D-CRT plus AST group vs. 57 percent in the 3D-CRT group." The researchers note there were 6 deaths due to prostate cancer and 17 from other causes for patients receiving 3D-CRT. For patients receiving 3D-CRT plus AST, no deaths occurred due to prostate cancer and 12 were from other causes.
"Given that many men treated for prostate cancer are often older and that AST use of more than one year has been shown to cause osteopenia, impairment of memory, attention and executive functions, and prolongation of the QT interval [heart rhythm], in addition to anemia, muscle loss in exchange for body fat, hot flashes, and impotence, minimizing these effects by decreasing AST duration could profoundly impact a patient's quality of life. Therefore, the clinically significant implication of our study is that a 6-month course of AST in patients receiving RT who have clinically localized prostate cancer may be sufficient to reduce the risk of death," the authors conclude.
(JAMA. 2004;292:821-827. Available post-embargo at jama.com)
EDITORIAL: COMBINATION THERAPY FOR PROSTATE CANCER
In an accompanying editorial, Theodore L. DeWeese, M.D., from The Johns Hopkins University School of Medicine, Baltimore, states: "One of every 6 men living in the United States will be diagnosed with prostate cancer at some point in his life. Although the likelihood of death from such a diagnosis is much less than 1 in 6, nearly 30,000 men will die from prostate cancer this year."
Concludes DeWeese, "...the study reported by D'Amico et al is important particularly in that it is the first to demonstrate a survival benefit when AST is added to RT in the management of patients with clinically localized prostate cancer. Based on the results of this compelling study, can one say that AST in combination with RT is now the 'standard' therapy for patients with clinically localized intermediate- to high-risk prostate cancer? ...Several important issues about the data set remain unclear and, when combined with the fact that the radiation doses used in this trial were lower than that shown to be beneficial for similar patients in other studies, the term 'standard' cannot yet be applied to this approach for all patients managed with RT for clinically localized prostate cancer."
(JAMA. 2004;292:864-866. Available post-embargo at jama.com)
For More Information: Contact the JAMA/Archives Media Relations Department at 312/464-JAMA (5262) or email: mediarelations{at}jama-archives.org
Go back to the top.
Embargoed for Release: 3 p.m. CT, TUESDAY, August 17, 2004
Media Advisory: To contact Simin Nikbin Meydani, D.V.M., Ph.D., call Peggy Hayes at 617-636-3707.
VITAMIN E SHOWS MIXED EFFECTS AGAINST RESPIRATORY INFECTIONS IN NURSING HOME RESIDENTS
Possible Effect on Common Cold Requires Further Study
CHICAGOVitamin E does not appear to have a beneficial effect on lower respiratory tract infections in elderly nursing home residents, but it may help them ward off upper respiratory tract infections, according to a study in the August 18 issue of JAMA, the Journal of the American Medical Association.
"Infections, particularly respiratory tract infections, are common in elderly individuals, resulting in decreased daily activity, prolonged recovery times, increased health care service use, and more frequent complications, including death," the authors provide in background information. "In the United States, an estimated 43 percent of elderly persons will be admitted to a nursing home, with more than 85 percent of them admitted to long-term (more than one year) care facilities. Infections occur more frequently in nursing home residents than among independent-living elderly..."
Simin Nikbin Meydani, D.V.M., Ph.D., from Tufts University, Boston, and colleagues enrolled 617 persons at least 65 years old in 33 long-term care facilities from April 1998 to August 2001 to participate in a clinical trial to determine the effect of one-year of vitamin E supplementation on respiratory tract infections in elderly nursing home residents. The study participants were randomized to two groups. All participants received a multivitamin capsule with 50 percent of the recommended daily allowance (RDA) for essential micronutrients. The vitamin E group (n = 311) received a daily capsule containing 200 international units (IU) of vitamin E and the control group (n = 306) received a placebo capsule. A total of 451 participants (73 percent) completed the study.
"Vitamin E had no significant effect on incidence or number of days with infection for all, upper, or lower respiratory infections. However, fewer participants receiving vitamin E acquired one or more respiratory tract infections (60 percent vs. 68 percent for all participants; and 65 percent vs. 74 percent for completing participants), or upper respiratory tract infections (44 percent vs. 52 percent for all participants; and 50 percent vs. 62 percent for completing participants)," the authors found. In analysis the authors had not planned before conducting the study, the researchers report that "participants in the vitamin E group who completed the study had significantly fewer common colds and a 20 percent lower risk of acquiring a cold than those in the placebo group."
"In conclusion, we found no effect of vitamin E supplementation on the incidence or duration of respiratory tract infections. However, significantly fewer vitamin E participants acquired one or more respiratory tract infections, which was more evident in URIs [upper respiratory tract infections]. Post hoc subgroup analysis among individuals completing the study revealed a significantly lower incidence of common cold and fewer participants acquiring a cold. Common colds are frequent and associated with increased morbidity in this age group, and if confirmed [in future studies], these findings suggest important implications for the well-being of the elderly."
(JAMA. 2004;292:828-836. Available post-embargo at jama.com)
Editor's Note: The research for this work was performed in the Nutritional Immunology Laboratory, Jean Mayer U.S. Department of Agriculture/HNRC at Tufts University, Boston, Mass. This work was supported by a grant from the National Institute on Aging (NIA), National Institutes of Health, and a Department of Agriculture agreement, and a grant for preparation of study capsules from Hoffman-LaRoche, Inc.
For More Information: Contact the JAMA/Archives Media Relations Department at 312/464-JAMA (5262) or email: mediarelations{at}jama-archives.org
Go back to the top.
JAMA VIDEO NEWS REPORT
FLUOXETINE PLUS COGNITIVE BEHAVIORAL THERAPY SUPERIOR FOR TREATING TEEN DEPRESSION COMPARED TO MEDICATION OR THERAPY ALONE
VIDEO:
B-ROLL
Kids shopping at mall (no faces showing)
Teen with mother
Teens
GFX/JAMA COVER
AUDIO:
TEEN DEPRESSION CAN HURT SCHOOL PERFORMANCE, RELATIONSHIPS WITH FAMILY
AND FRIENDS, AND EVEN LEAD TO SUICIDE. A NEW STUDY IN JAMA, THE JOURNAL
OF THE AMERICAN MEDICAL ASSOCIATION, COMPARED DEPRESSION TREATMENT
METHODS IN TEENS.
VIDEO:
SOT/FULL @ : 13
Super: John March, M.D., M.P.H., Treatment for Adol. with Depression Study
Runs :09
AUDIO:
"We also wanted to see if there was advantage to combining the
treatments over using the individual treatments alone."
VIDEO:
B-ROLL
Dr. March looking over journal
Fluoxetine tablets
More teen
AUDIO:
DR. JOHN MARCH AT DUKE UNIVERSITY MEDICAL CENTER IS PART A GROUP OF
PSYCHIATRISTS AND PSYCHOLOGISTS WHO DESIGNED THE "TREATMENT FOR
ADOLESCENTS WITH DEPRESSION STUDY." THE RESEARCHERS ENROLLED 439
MODERATELY TO SEVERELY DEPRESSED TEENS AT THIRTEEN SITES ACROSS THE
COUNTRY. SOME OF THE TEENS WERE TREATED WITH THE ANTI-DEPRESSANT
FLUOXETINE (flu-OX-eh-teen), SOME WERE TREATED WITH COUNSELING CALLED
COGNITIVE BEHAVIORAL THERAPY, OR CBT. SOME RECEIVED A COMBINATION OF
FLUOXETINE AND CBT, AND SOME GOT PLACEBO, OR SUGAR PILL. AFTER 12 WEEKS
OF TREATMENT, HERE'S WHAT THE RESEARCHERS FOUND.
VIDEO:
SOT/FULL
John March, M.D., M.P.H., Treatment for Adol. with Depression Study
Runs :06
AUDIO:
"The combination of the two treatments, Fluoxetine and cognitive
behavioral psychotherapy, has a significant advantage."
VIDEO:
B-ROLL
FULL SCREEN GRAPHIC
Title: Treatment for Adolescents with Depression Study
71% on combination therapy improved
43% in counseling alone improved
35% on placebo improved
61% on fluoxetine improved
AUDIO:
ABOUT 70 PERCENT OF KIDS RECEIVING COMBINATION THERAPY RESPONDED TO
TREATMENT. ABOUT 40 PERCENT OF TEENS RECEIVING COUNSELING ALONE
RESPONDED. 35 PERCENT OF TEENS ON PLACEBO SAW IMPROVEMENT. ABOUT 60 PERCENT OF
TEENS TAKING FLUOXETINE ALONE RESPONDED... CLOSE TO THE RESPONSE RATE
OF THOSE RECEIVING COMBINED THERAPY. BUT THERE WAS AN IMPORTANT
DIFFERENCE.
VIDEO:
SOT/FULL
John March, M.D., M.P.H., Treatment for Adol. with Depression Study
Runs :07
AUDIO:
"There seems to be an increased risk of doing something harmful to
yourself if you're treated with medication as compared to being treated
with CBT."
VIDEO:
B-ROLL
Fluoextine pills
Pharmacy tech counting pills
AUDIO:
IN OTHER WORDS, FLUOXETINE DID IMPROVE DEPRESSION, BUT KIDS TAKING IT
STILL HAD A SLIGHTLY HIGHER RISK OF SELF-HARM. CBT, OR COUNSELING,
SEEMS TO MITIGATE THAT RISK.
VIDEO:
SOT/FULL
John March, M.D., M.P.H., Treatment for Adol. with Depression Study
Runs :13
AUDIO:
"The treatments target different things. It's likely that fluoextine
targets the broad domain of regulation of mood and feelings, whereas CBT
targets specific domains like suicidal thinking or family conflict."
VIDEO:
B-ROLL
Teens
AUDIO:
THAT COMBINATION APPEARS TO BE THE MOST EFFECTIVE WAY TO TREAT
ADOLESCENT DEPRESSION.
THIS IS MAVIS PRALL REPORTING.